"
Team:Paris Saclay/Notebook/August/6
From 2013.igem.org
(Difference between revisions)
(→1 - Electroelution of BBa_I732017 digested by EcoRI/SpeI) |
(→Objective : obtaining biobricks in PSB3K3) |
||
| Line 98: | Line 98: | ||
|} | |} | ||
| - | ===='''Objective : obtaining biobricks in | + | ===='''Objective : obtaining biobricks in pSB3K3'''==== |
====1 - Extraction of BBa_J04450 from DH5α==== | ====1 - Extraction of BBa_J04450 from DH5α==== | ||
Revision as of 17:38, 3 October 2013
Notebook : August 6
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining BBa_K1155004, BBa_K1155005, BBa_K1155006
1 - Electrophoresis to check the Colony PCR products : BBa_K1155004, BBa_K1155005, BBa_K1155006
XiaoJing, Damir, Anaïs
- BBa_K1155004 :
 
|
|
- BBa_K1155005 :
 
|
|
- BBa_K1155006 :
|
|
Expected size :
- NarK, NarG, NirB : 500 bp
|
We obtain fragments at the good size for all the colony. We will make a culture of DH5α with BBa_K1155004, BBa_K1155005 and BBa_K1155006. We will also sequence our plasmids. |
2 - Liquid culture of DH5α with BBa_K1155004, BBa_K1155005 and BBa_K1155006
Xiaoing, Anaïs
Used quantities :
- LB : 5mL
- Chloramphénicol (1000X, 20µg/mL) : 5µL
- BBa_K1155004, BBa_K1155005 and BBa_K1155006 : 25µL
We let the incubation over night at 37°C at 180 RPM.
We used colonies number 6, 7 and 8 for each promotor.
Objective : obtaining BBa_K1155007
1 - Electroelution of BBa_I732017 digested by EcoRI/SpeI
Nadia
Protocol : Electroelution
|
The electroelution was good. We will ligate RBS-LacZ with Term and pSB1C3. |
Objective : obtaining biobricks in pSB3K3
1 - Extraction of BBa_J04450 from DH5α
Abdou
Protocol : Low copy plamid extraction
B - PCB sensing system
Objective : obtaining BBa_K1155002
1 - Sequence analysis for BBa_K1155002 in clones 4, 17 and 22
|
The sequence is good for each clone. We obtain a new biobrick : BBa_K1155002. |
| Previous day | Back to calendar | Next day |
